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Hemoglobin
international journal for hemoglobin research
Volume 28, 2004 - Issue 2
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Short Communication

Thalassemia Intermedia Due to Co‐inheritance of β0/β+‐Thalassemia and (– –SEA) α‐Thalassemia/Hb Westmead [α122(H5)His > Gln (α2)] in a Chinese Family

Wai‐Shan Wong Division of Hematology, Department of Pathology, The University of Hong Kong, Queen Mary Hospital, 102 Pokfulam Road, Hong Kong, P.R. of China
,
Amy Y‐Y. Chan Division of Hematology, Department of Pathology, The University of Hong Kong, Queen Mary Hospital, 102 Pokfulam Road, Hong Kong, P.R. of China
,
Sze‐Fai Yip Department of Medicine, Tuen Mun Hospital, Hong Kong, P.R. of China
&
Edmond Shiu‐Kwan Ma Division of Hematology, Department of Pathology, The University of Hong Kong, Queen Mary Hospital, 102 Pokfulam Road, Hong Kong, P.R. of China
Pages 151-156 | Received 22 Nov 2003, Accepted 03 Dec 2003, Published online: 24 Aug 2009

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Philippe Joly, Caroline Garcia, Philippe Lacan, Nicole Couprie & Alain Francina. (2011) Two New Hemoglobin Variants: Hb Aix-Les-Bains [β5(A2)Pro→Leu; HBB:c.17 C>T] and Hb Dubai [α122(H5)His→Leu (α2); HBA2:c.368 A>T]. Hemoglobin 35:2, pages 147-151.
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Noppacharn Uaprasert, Rung Settapiboon, Supaporn Amornsiriwat, Pranee Sutcharitchan & Ponlapat Rojnuckarin. (2017) The first validated criteria for effective screening and a new simplified method for α-globin gene sequencing for diagnosis of uncommon α-globin mutations. International Journal of Hematology 105:6, pages 819-827.
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Michela Grosso, Stella Puzone, Maria Rosaria Storino, Raffaele Sessa & Paola Izzo. (2013) Prenatal diagnosis of haemoglobinopathies: our experience of 523 cases. Clinical Chemistry and Laboratory Medicine (CCLM) 51:12, pages 2219-2225.
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María Paulina Nava, Bertha Ibarra, María Teresa Magaña, María de la Luz Chávez & F. Javier Perea. (2006) Prevalence of −α3.7 and αααanti3.7 alleles in sickle cell trait and β-thalassemia patients in Mexico. Blood Cells, Molecules, and Diseases 36:2, pages 255-258.
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